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Aquaporins Production Optimization and Characterization THESIS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN NATURAL SCIENCE AQUAPORINS PRODUCTION OPTIMIZATION AND CHARACTERIZATION FREDRIK ÖBERG Department of Chemistry – Biochemistry Göteborg, Sweden 2011 Thesis for the Degree of Doctor of Philosophy in Natural Science AQUAPORINS: Production Optimization and Characterization Fredrik Öberg Cover: Cells of the yeast Pichia pastoris, producing hAQP5 fused to green fluorescence protein. Visualized using confocal microscopy. Copyright © 2011 by Fredrik Öberg ISBN 978-91-628-8290-7 Available online at http://hdl.handle.net/2077/25277 Department of Chemistry Biochemistry and Biophysics SE-413 90 Göteborg, Sweden Printed by Chalmers Reproservice Göteborg, Sweden 2011 Till min familj ABSTRACT Aquaporins are water facilitating proteins embedded in the cellular membranes. Such channels have been identified in almost every living organism – including humans. They are vital molecules and their malfunction can lead to several severe disorders. An increased understanding of their structure, function and regulation is of utmost importance for developing current and future drugs. The first problem to overcome is to acquire the proteins in sufficient amounts to enable characterization. To achieve this, proteins are often produced in a host organism. One of the most successful hosts for recombinant overproduction is the yeast Pichia pastoris. Using this yeast we could obtain exceptional yield of aquaporin 1, whereas some others were below the threshold needed for successful subsequent characterization. In this process, we have established methods allowing fast and accurate determination of the initial production yield. Furthermore, we optimized the yield for low producing targets, enabling studies of proteins previously out of reach, exemplified with human aquaporin 4. Characterization has been performed on aquaporins obtained in sufficient quantities, and the functionality of aquaporin 1, 5 and 10 has been assessed. Furthermore, a glycosylation was found to stabilize the aquaporin 10 tetramer although only a minority of the monomers where modified. Moreover, we used protein crystallography to determine the three dimensional structure of a hAQP5 mutant, providing insight into regulation of the protein by trafficking. Taken together, these results provide insight into factors directing high production of eukaryotic membrane proteins. The subsequent characterization, including functional and structural determination, reveals new knowledge about aquaporin activity and regulation. LIST OF PUBLICATIONS This thesis is based on the following papers listed in reverse chronological order. They are appended at the end of the thesis and will be referred to in the text by their roman numerals. Paper I. Nyblom, M., Öberg, F., Lindkvist-Petersson, K., Hallgren, K., Findlay, H., Wikström, J., Karlsson, A., Hansson, Ö., Booth, P. J., Bill, R. M., Neutze, R. and Hedfalk, K. (2007) Exceptional overproduction of a functional human membrane protein. Protein Expr Purif, 56, 110-20. Paper II. Hedfalk, K., Pettersson, N., Öberg, F., Hohmann, S. and Gordon, E. (2008) Production, characterization and crystallization of the Plasmodium falciparum aquaporin. Protein Expr Purif, 59, 69-78. Paper III. Öberg, F., Ekvall, M., Nyblom, M., Backmark, A., Neutze, R. and Hedfalk, K. (2009) Insight into factors directing high production of eukaryotic membrane proteins; production of 13 human AQPs in Pichia pastoris. Mol Membr Biol, 1-13. Paper IV. Öberg, F., Sjöhamn, J., Conner, M.T., Bill, R.M., Hedfalk, K. (2011) Improving recombinant eukaryotic membrane protein yields in Pichia pastoris: the importance of codon optimisation and clone selection. Submitted Paper V. Öberg, F., Sjöhamn, J., Fischer, G., Moberg, A., Pedersen, A., Neutze, R., Hedfalk, K. (2011) Glycosylation increases the thermostability of human aquaporin 10. Submitted Paper VI. Öberg, F., Sjöhamn, J., Hedfalk, K., Neutze, R., Törnroth-Horsefield, S. (2011) Crystal structure of the S156E-mutant of human aquaporin 5. Manuscript. Related publication Paper VII. Wöhri, A. B., Johansson, L. C., Wadsten-Hindrichsen, P., Wahlgren, W. Y., Fischer, G., Horsefield, R., Katona, G., Nyblom, M., Öberg, F., Young, G., Cogdell, R. J., Fraser, N. J., Engström, S. and Neutze, R. (2008) A lipidic-sponge phase screen for membrane protein crystallization. Structure, 16, 1003-9. CONTRIBUTION REPORT There are multiple authors on the papers presented here and my contribution to each of them is listed below. The focus of my thesis is on areas where I have made major contributions. Paper I. I was involved in planning the project and cloned the tagged construct, screened for protein production, and performed optimization and production experiments. I was involved in data processing and analysis as well as manuscript preparation. Paper II. I was involved in planning the project and cloned the constructs for production in Pichia pastoris. I was involved in data analysis, figure preparations, and writing of the manuscript. Paper III. I planned the project and was responsible for cloning the constructs, protein production, quantitation, and localization studies. I took a major part in interpretation of the results, preparing figures, and writing of the manuscript. Paper IV. I was involved in planning the project and was responsible for designing the cloning of the constructs, transformation, protein production, quantitation, Zeocin screens, and preparing figures. I took part in the localization studies with GFP, interpretation of the results, and writing of the manuscript. Paper V. I planned the project and was responsible for cloning the constructs, producing and purifying the protein, glycosylation studies, circular dichroism, crystallization, and functional studies using stopped-flow. I took a major part in interpretation of the results, preparing figures, and writing of the manuscript. Paper VI. I planned the project and was responsible for cloning the constructs, producing and purifying the protein, crystallization, collecting diffraction data, structure determination, structure refinement, and figure preparation. I took part in the interpretation of the structure and writing of the manuscript. CONTENTS 1 INTRODUCTION ........................................................................................ 1 1.1 Proteins – Unique Structural Elements .............................................................................. 1 1.2 Membrane proteins – Fundamental Molecules of Life ....................................................... 1 1.3 Recombinant Production of Membrane Proteins ............................................................... 2 1.4 Pichia pastoris as Production Host ..................................................................................... 4 1.4.1 From Discovery to Current Use ..................................................................................................... 5 1.4.2 Strength in Protein Production ....................................................................................................... 5 1.5 Protein Glycosylation - Modification of Proteins ................................................................ 6 1.5.1 N-linked Glycosylation ..................................................................................................................... 7 1.5.2 N-linked Glycosylation in Pichia pastoris ......................................................................................... 9 1.5.3 Biological Relevance of N-linked Glycosylation .......................................................................... 9 1.6 Water and Aquaporins ....................................................................................................... 10 1.6.1 Discovery of Aquaporins ............................................................................................................... 10 1.6.2 Structural Features ........................................................................................................................... 11 1.7 Human Aquaporins ........................................................................................................... 13 1.7.1 Aquaporin 0 ...................................................................................................................................... 13 1.7.2 Aquaporin 1 ...................................................................................................................................... 14 1.7.3 Aquaporin 2 ...................................................................................................................................... 14 1.7.4 Aquaporin 3 ...................................................................................................................................... 14 1.7.5 Aquaporin 4 ...................................................................................................................................... 15 1.7.6 Aquaporin 6 ...................................................................................................................................... 15 1.7.7 Aquaporin 7 ...................................................................................................................................... 16 1.7.8 Aquaporin 8 ...................................................................................................................................... 16 1.7.9 Aquaporin 9 .....................................................................................................................................
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